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- 上海
- 2026年05月23日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
期货
- 英文名：
Ethyl 2-amino-3-(1H-imidazol-5-yl)propanoate
- CAS号：
184295-36-1
- 供应商：
上海阿拉丁生化科技股份有限公司
- 保存条件：
室温
- 规格：
E1015676-1g
中文名：Ethyl 2-amino-3-(1H-imidazol-5-yl)propanoate
英文名：Ethyl 2-amino-3-(1H-imidazol-5-yl)propanoate
纯度：≥97%
货号：E1015676
Cas号：184295-36-1
存储温度：室温
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文献和实验Preparation of Unnatural Amino Acids with Ammonia-Lyases and 2,3-Aminomutases
of unnatural amino acids. Besides the synthesis of various unnatural α-amino acids with the aid of phenylalanine ammonia-lyases (PALs) utilizing the 3,5-dihydro-5-methylidene-4H-imidazol-4-one (MIO) prosthetic groups, the biotransformations leading to various
Synthesis of 3-Amino-l-CarboxymethyI-Benzodiazepine (BZA) Peptidomimetics
inhibitors of Ras famesyltransferase (FTase) (6 ,7 ). The central pair of amino acids in the CAAX tetrapeptide was replaced with the nonpeptide scaffold 3-methylamino-1-carboxymethyl-2,3-dihydro-5-phenyl-1H-1,4-benzodiazepin-2-one, (N -Me)BZA, shown below.
Synthesis and Application of Highly Reactive Amino Linkers for Functional Oligonucleotides
are functionalized by conjugation with a variety of molecules, and aliphatic amino linkers have been frequently used as a tether for their modifications. This unit describes the syntheses and applications of novel amino linkers having a carbamate structure
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